One‐year outcomes of pulmonary vein isolation with a novel cryoballoon: Primary results of the FROZEN AF trial

Author:

Ellenbogen Kenneth A.1,Mittal Suneet2,Varma Niraj3ORCID,Aryana Arash4ORCID,Marrouche Nassir5ORCID,Anić Ante6,Nair Devi7,Champagne Jean8,Iacopino Saverio9ORCID,de Asmundis Carlo10,Weiner Stanislav11,Makati Kevin12,Raybuck Jonathan D.13,Richards Elizabeth13,Su Wilber14ORCID

Affiliation:

1. Division of Cardiology Virginian Commonwealth University Richmond Virginia USA

2. Valley Hospital Ridgewood New Jersey USA

3. Cleveland Clinic Cleveland Ohio USA

4. Mercy General Hospital Sacramento California USA

5. Tulane University School of Medicine New Orleans Louisiana USA

6. University Hospital Split Split Croatia

7. Arrhythmia Research Group Jonesboro Arkansas USA

8. Institut Universitaire de Cardiologie et de Pneumologie de Quebec Quebec Canada

9. Maria Cecilia Hospital Cotignola Italy

10. UZ Brussel Brussels Belgium

11. Christus Trinity Mother Frances Health System Tyler Texas USA

12. St. Joseph's Hospital Tampa Florida USA

13. Boston Scientific Arden Hills Minnesota USA

14. Banner University Medical Center Phoenix Arizona USA

Abstract

AbstractIntroductionCryoablation therapy for pulmonary vein isolation (PVI) to treat paroxysmal atrial fibrillation (PAF) is well established. A novel 28 mm cryoballoon system designed to operate under low pressure to safely reach a lower nadir temperature and maintain constant balloon size during cooling has not been prospectively studied in a large patient population for safety and efficacy. The FROZEN AF (NCT04133168) trial was an international multicenter, open‐label, prospective, single‐arm study on the safety and performance of a novel cryoballoon system for treatment of PAF.Methods and ResultsThe study enrolled patients at 44 sites in 10 countries across North America, Europe, and Asia. Subjects were indicated for PVI treatment of PAF and had failed or were intolerant of one or more antiarrhythmic drugs. Procedural outcomes were defined based on the 2017 HRS consensus statement. Follow‐up was performed at 7 days, 3, 6, and 12 months. Data are reported as mean ± SD or median (IQR). PVI was performed with a 28 mm cryoballoon in 325 drug refractory PAF patients. Complete PVI was achieved in 95.7% of patients. In cryoablation lesions longer than 60 s, 60.1% of PV isolations required only a single cryoballoon application. Procedure related complications included: phrenic nerve palsy [temporary 4 (1.2%), persistent 0 (0.0%)], cardiac tamponade/perforation 2 (0.6%), and air embolism 1 (0.3%). Freedom from documented atrial arrhythmia recurrence at 12 months was 79.9% (AF 82.7%, AFL 96.5%, AT 98.1%), antiarrhythmic drugs (AAD) were continued or re‐initiated in 26.8% of patients after the 3‐month blanking period. Additionally, an extension arm enrolled 50 pts for treatment with 28/31 mm variable size cryoballoon. A single temporary PNP occurred in this group, which resolved before discharge. Freedom from documented recurrence at 12 months in these pts was 82.0%.ConclusionsThis novel cryoballoon may facilitate PVI to treat PAF, providing more options to address the variety of anatomies present in patients with PAF. This cryoballoon system proved to be safe and effective for treatment of patients with drug refractory or drug intolerant PAF.

Funder

Boston Scientific Corporation

Publisher

Wiley

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